Results 281 to 290 of about 3,626,748 (297)

Expansion of the Structure-Activity Relationship Profile of Triaminopyrimidines as Inhibitors of Caspase-1. [PDF]

open access: yesChem Biol Drug Des
East A   +8 more
europepmc   +1 more source

Enhancing Fatigue Performance by Tuning of Residual Stresses in Welded Joints through Nanometallic Multilayer

open access: yesAdvanced Engineering Materials, EarlyView.
This study investigates the fundamental mechanisms of a novel postweld treatment that significantly enhances fatigue performance through engineered residual stress (RS) states. A multiscale approach correlates tensile RS in the nanometallic multilayer coating with corresponding compressive RS in the steel substrate, thereby reducing localized stress ...
Niclas Spalek   +3 more
wiley   +1 more source

Identification of a New FtsZ Inhibitor by Virtual Screening, Mechanistic Insights, and Structure-Activity Relationship Analyses. [PDF]

open access: yesACS Infect Dis
Sciò P   +13 more
europepmc   +1 more source

Four‐Point Bending Tests at High Temperatures on Commercial MgO‐C Refractory Bricks with and Without Recyclate Considering Different Carbon Contents

open access: yesAdvanced Engineering Materials, EarlyView.
Four‐point bending tests are conducted in an argon atmosphere on commercial MgO‐C brick grades with and without MgO‐C recyclate from room temperature up to 1300 °C. No detrimental effect of the MgO‐C recyclates on bending strength is found. Instead, a decisive influence of the total carbon content is observed, with lower total carbon contents ...
Alexander Schramm   +5 more
wiley   +1 more source

α-Glucosidase Inhibitors from the Leaves of <i>Cannabis sativa</i>: Structure-Activity Relationship, Kinetic Investigation, and Molecular Docking. [PDF]

open access: yesJ Agric Food Chem
Nguyen AK   +6 more
europepmc   +1 more source

Correction to "Structure-Activity Relationship Studies of the Peptide Antibiotic Clovibactin". [PDF]

open access: yesJ Org Chem
Brunicardi JEH   +7 more
europepmc   +1 more source

Discovery of highly potent naphthalene/quinoline-based PAD inhibitors: Structure-activity relationship, selectivity, and cytotoxicity. [PDF]

open access: yesEur J Med Chem
Jia Y   +9 more
europepmc   +1 more source

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